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Comprehensive Study of the Clinical Phenotype of Germline BAP1 Variant-Carrying Families Worldwide S Walpole, AL Pritchard, CM Cebulla, R Pilarski, M Stautberg, ... JNCI: Journal of the National Cancer Institute 110 (12), 1328-1341, 2018 | 237 | 2018 |
Genome-wide scan in a nationwide study sample of schizophrenia families in Finland reveals susceptibility loci on chromosomes 2q and 5q T Paunio, J Ekelund, T Varilo, A Parker, I Hovatta, JA Turunen, K Rinard, ... Human molecular genetics 10 (26), 3037-3048, 2001 | 198 | 2001 |
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Latent autoimmune diabetes in adults differs genetically from classical type 1 diabetes diagnosed after the age of 35 years MK Andersen, V Lundgren, JA Turunen, C Forsblom, B Isomaa, PH Groop, ... Diabetes care 33 (9), 2062-2064, 2010 | 125 | 2010 |
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Further evidence for linkage of autosomal-dominant medullary cystic kidney disease on chromosome 1q21 M Auranen, S Ala-Mello, JA Turunen, I Järvelä Kidney international 60 (4), 1225-1232, 2001 | 52 | 2001 |
Association analysis of the AIRE and insulin genes in Finnish type 1 diabetic patients JA Turunen, M Wessman, C Forsblom, R Kilpikari, M Parkkonen, ... Immunogenetics 58, 331-338, 2006 | 50 | 2006 |
Genetic risk factors associated with preeclampsia and hypertensive disorders of pregnancy JS Tyrmi, T Kaartokallio, AI Lokki, T Jääskeläinen, E Kortelainen, ... JAMA cardiology 8 (7), 674-683, 2023 | 49 | 2023 |
BAP1 germline mutations in Finnish patients with uveal melanoma JA Turunen, S Markkinen, R Wilska, S Saarinen, V Raivio, M Täll, ... Ophthalmology 123 (5), 1112-1117, 2016 | 49 | 2016 |
RHD maternal–fetal genotype incompatibility and schizophrenia: extending the MFG test to include multiple siblings and birth order P Kraft, CGS Palmer, AJ Woodward, JA Turunen, S Minassian, T Paunio, ... European journal of human genetics 12 (3), 192-198, 2004 | 49 | 2004 |
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Keratoendotheliitis fugax hereditaria: a novel cryopyrin-associated periodic syndrome caused by a mutation in the nucleotide-binding domain, leucine-rich repeat family, pyrin … JA Turunen, J Wedenoja, P Repo, RS Järvinen, JE Jäntti, S Mörtenhumer, ... American journal of ophthalmology 188, 41-50, 2018 | 41 | 2018 |
Linkage and linkage disequilibrium scan for autism loci in an extended pedigree from Finland H Kilpinen, T Ylisaukko-oja, K Rehnström, E Gaál, JA Turunen, E Kempas, ... Human molecular genetics 18 (15), 2912-2921, 2009 | 41 | 2009 |
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